#44885 05-07-2005 08:22 AM | Joined: Mar 2005 Posts: 14 Member | OP Member Joined: Mar 2005 Posts: 14 | maybe not doing this correctly.....need some info re: foods to start on after treatment. Dave is 1 month out and not having a terrible time with the salivary glands not working. Does anyone have any input as to what helped them if they were in this similar position. Had 35 rad and 3 cycles cisplatin. G-tube for feeding. No real food now for about 2 1/2 months. Need some help....He desperately wants to eat and I have no suggestions. Please Help.....  | | |
#44886 05-07-2005 05:52 PM | Joined: Nov 2002 Posts: 3,552 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Nov 2002 Posts: 3,552 | Patience! At 1 month his radiation side effects are just now starting to subside. It can take 18 months or more for salivary function to return (if he had IMRT). The taste buds should start working again slowly as well. The food thing was one of the worst parts for me.
Gary Allsebrook *********************************** Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2 Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy) ________________________________________________________ "You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
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#44887 05-08-2005 05:50 AM | Joined: Mar 2003 Posts: 1,384 Likes: 1 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Mar 2003 Posts: 1,384 Likes: 1 | Tammy, Buy or borrow a blender and put anything in it. Add some milk or gravy and you can turn any meal into something he can eat without saliva. If you search "blender" here you should come up with more on this including recipies. E-mail me and I will send more information.
Take care
Mark, 21 Year survivor, SCC right tonsil, 3 nodes positive, one with extra-capsular spread. I never asked what stage (would have scared me anyway) Right side tonsillectomy, radical neck dissection right side, maximum radiation to both sides, no chemo, no PEG, age 40 when diagnosed.
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#44888 05-09-2005 01:30 AM | Joined: Aug 2004 Posts: 100 Gold Member (100+ posts) | Gold Member (100+ posts) Joined: Aug 2004 Posts: 100 | Tammy, Gary is so right! Patience.My friend Rod had the same tx as Dave. As soon as tx was over, he thought he could start eating everything!Wrong! He started with scrambled eggs, mashed potatoes & gravy and soup and that was about it for a while. He just started experimenting for a while and by about 5 months after tx, he was doing so much better!  Even now, 10 months after tx stopped, he is finally getting a little saliva & is able to eat pizza! Try to watch his progress weekly instead of daily, someone told us that & it made a huge difference. Tell him it is a slow recovery process & it will get better with patience. God bless & let me know if I can help! God bless!Maureen
maureen (friend to Rod SCC tonsil diag. Mar 04 stage 4 -concurrent rad. & chemo) Finished tx July 04
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#44889 05-09-2005 04:32 AM | Joined: Feb 2004 Posts: 261 Gold Member (200+ posts) | Gold Member (200+ posts) Joined: Feb 2004 Posts: 261 | You just have to experiment, but don't give up. I can eat anything with enough milk to wash it down. Obviously some things are easier than others. Lean meats are the hardest. Lots of butter! Chicken burger with extra tomato & extra mayo - no lettuce. If he can chew it, it's pretty slippery & goes down with milk. Lots of strong coffee w/cream & sugar seems to coat the mouth & throat. Tomatoes w/everything. I eat a lot healthier these days because alot of processed foods are hard to manage. Steamed veggies w/lots of butter. Steamed squash w/lots of butter & tomatoe, diced onion, basil,salt & olive oil salad! Delicious! Get creative. I love ice cream & I keep eating it but it always makes me cough! You just have to figure out what works. It gets easier with time. Never give up.
dx 2/11/04 scca bot T3 IU 2B MO poorly differentiated, margins ok, 3/16 modest, jaw split, over half of tongue removed, free flap from left forearm - finished chemo & rad treatment 5/20/04
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#44890 05-09-2005 05:33 AM | Joined: Mar 2003 Posts: 251 Gold Member (200+ posts) | Gold Member (200+ posts) Joined: Mar 2003 Posts: 251 | Have to second Erik's suggestions. My husband found that tomatoes really helped get foods down. Also, blender stuff didn't work so well for him (but everybody is different, of course). He's 2 years post treatment and, just within the last few months is able to drink milkshakes or smoothies without them sending him into a coughing fit.
There are some good "non-chew" cookbooks out there. The one I bought and used (and still use) is "I-Can't-Chew Cookbook" by J. Randy Wilson. Subtitle is "Delicious soft-diet recipes for people with chewing, swallowing and dry-mouth disorders."
Anita
Husband Dx 12/02 Stage 4 Tonsil Cancer T1N2bM0; surgery, radiation, chemo 1/03 - 4/03.
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#44891 05-09-2005 02:25 PM | Joined: Mar 2005 Posts: 14 Member | OP Member Joined: Mar 2005 Posts: 14 | thank you everyone for your input we greatly appreciate it. I am sure that it is going to be a long haul..we'll truck along. you are all such wonderful people I am so greatful to have found you. Thanks for all the support..God bless Tammy | | |
#44892 05-28-2005 06:09 AM | Joined: Mar 2005 Posts: 6 Member | Member Joined: Mar 2005 Posts: 6 | Tammy, I was in a similar situation post radiation. My throat pain has finally improved enough that I started to eat some food by mouth, but it is hit and miss.
First I started with soft foods that I could swallow easily and not gag. What I do is keep a list of foods that still have some taste and try to keep to the list.
Some of the items on my list are: noodles, crackers broken up in a bowl of soup, cheese, whole milk, sliced canned peaches, bananas, peanut butter and jelly sandwiches, and spagetti with just plain sauce no meat.
I still do tube feedings generally 6 Boost plus a day as well as what I can get in orally.
Hope this helps.
Morris | | |
#44893 05-28-2005 03:04 PM | Joined: Jul 2003 Posts: 1,163 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Jul 2003 Posts: 1,163 | Hello Tammy,
When I started eating again I started with soups. They slide right down. Smoothies are also easy to eat and have lots of calories and protien. Like eating a milkshake. Your choice of flavor on the ice cream & carnation instant Breakfast.
Smoothie: 1 Cup Whole Milk 1/2 Cup Half & Half 1-1/2 oz. Whey Protein Powder (GNC) 1 package Carnation Instant Breakfast 2 cups Ice Cream 1 Tablespoon Malted Milk. (powder)
Mix in blender and serve in a frosted mug. Each one is about 1400 calories. I cut the receipe in half and one is around 800 calories and about 42% of his daily protein needs. Also the half fills a 16 oz. mug right to the top. They taste good. There is light at the end of the tunnel, It justs takes us awhile to get there. Dave will be there soon.
Best Wishes, Danny Boy
Daniel Bogan DX 7/16/03 Right tonsil,SCC T4NOMO. right side neck disection, IMRT Radiation x 33.
Recurrance in June 05 in right tonsil area. Now receiving palliative chemo (Erbitux) starting 3/9/06
Our good friend and loved member of the forum has passed away RIP Dannyboy 7-16-2006
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